Avacare is looking to solve the problem of managing clinical research trials by hiring a Clinical Research Coordinator to gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.
Requirements
- Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens
- Solid understanding of site operations and the drug development process
- Comfortable using CTMS, eCRFs, and Microsoft Office tools
Responsibilities
- Manage 2–6 trials of varying complexity
- Perform clinical procedures
- Lead study coordination from start to finish
- Obtain vital signs
- Perform phlebotomy
- Conduct ECGs
- Process lab specimens
Other
- Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants (CRC I)
- Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants (CRC II)
- Strong written and verbal communication skills, with attention to detail and time management
- Must be able to work on-site in Pleasant View, Utah
- Must be eligible to work in the United States
